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chemical reaction
mechanism
organic chemistry
deprotonation
synthesis
The image depicts an organic chemistry reaction mechanism. It begins with a cyclic ketone undergoing deprotonation at the alpha-carbon using a base, followed by alkylation with methyl iodide (MeI) to add a methyl group. The reaction is repeated with excess potassium hydride (KH) and MeI, adding two more methyl groups. Finally, the ketone undergoes a reaction with sodium amide (NaNH2) in ether (Et2O) to form an allylic double bond. The final product is an unsaturated cyclic ketone.
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